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Catalog Number:
23522
CAS Number:
602307-22-2
4-[3,5-Bis(trifluoromethyl)phenyl]benzaldehyde
Synonym(s):
3',5'-Di-(trifluoromethyl)-biphenyl-4-carbaldehyde
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$117.78 /250MG
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Product Information

4-[3,5-Bis(trifluoromethyl)phenyl]benzaldehyde is a highly specialized aromatic aldehyde known for its unique trifluoromethyl substituents, which enhance its reactivity and stability in various chemical applications. This compound is particularly valuable in the synthesis of advanced materials and pharmaceuticals, where its distinctive electronic properties can be leveraged to create compounds with improved efficacy. Researchers and industry professionals utilize this compound in the development of agrochemicals, dyes, and as a key intermediate in organic synthesis, enabling the production of complex molecular architectures. Its ability to participate in diverse chemical reactions, including nucleophilic additions and condensation reactions, makes it a versatile building block in synthetic chemistry.

Moreover, the trifluoromethyl groups confer unique characteristics that can improve the solubility and bioavailability of the resulting compounds, making them more effective in their applications. This compound stands out in the field of medicinal chemistry, where it can be used to design novel therapeutic agents with enhanced pharmacological profiles. With its broad applicability and significant advantages over similar compounds, 4-[3,5-Bis(trifluoromethyl)phenyl]benzaldehyde is an essential resource for researchers and manufacturers aiming to innovate and optimize their chemical processes.

Synonyms
3',5'-Di-(trifluoromethyl)-biphenyl-4-carbaldehyde
CAS Number
602307-22-2
Molecular Formula
C15H8F6O
Molecular Weight
318.22
MDL Number
MFCD02684111
PubChem ID
3863754
Conditions
Store at 0-8°C
General Information
Synonyms
3',5'-Di-(trifluoromethyl)-biphenyl-4-carbaldehyde
CAS Number
602307-22-2
Molecular Formula
C15H8F6O
Molecular Weight
318.22
MDL Number
MFCD02684111
PubChem ID
3863754
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-[3,5-Bis(trifluoromethyl)phenyl]benzaldehyde is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Material Science: It is used in the formulation of advanced materials, including polymers and coatings, due to its unique electronic properties and stability.
  • Fluorinated Compounds Research: The trifluoromethyl groups enhance the lipophilicity of compounds, making it valuable in drug design and discovery, particularly for targeting specific biological pathways.
  • Analytical Chemistry: This chemical acts as a standard in analytical methods, helping researchers calibrate instruments and validate techniques for detecting similar compounds.
  • Environmental Chemistry: It is studied for its behavior and degradation in various environments, aiding in the assessment of the environmental impact of fluorinated compounds.

Citations